Indolopyridines with a hetero atom at a position of fusion. 8. Reductive C-alkylation of indolo[2,1-<i>a</i>]isoquinolone

Authors

  • C. А. Солдатова Russian University of National Friendship, Moscow 117198
  • Х. А. Р. Аларкон Russian University of National Friendship, Moscow 117198
  • Ж. А. Мамырбекова Russian University of National Friendship, Moscow 117198
  • Л. И. Крывенко Russian University of National Friendship, Moscow 117198
  • Ж. Нтаганда Russian University of National Friendship, Moscow 117198
  • M. А. Ряшенцева Russian University of National Friendship, Moscow 117198

Abstract

Indolo(2,1-a]isoquinoline was alkylated at C(11) under catalytic hydrogenation conditions over rhenium heptasulfide in a medium of various alcohols. It was shown that the alkylation occurs by an electrophilic substitution mechanism and the yield of the products increases with decreasing acidity of the alcohols.

How to Cite
Soldatova, S. A.; Alarkon, J. A.; Mamyrbekova, Z. A.; Kryvenko, L. I.; Ntaganda, Dz.; Ryashetseva, M. A. Chem. Heterocycl. Compd. 1994, 30, 331. [Khim. Geterotsikl. Soedin. 1994, 377.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01165700

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Published

1994-03-25

Issue

No. 3 (1994)

Section

Original Papers